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HCID 13970723, 화합물 → 1-Nitro-2-(3,4-dimethoxyphenyl)cyclohexane

HRID 361305
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HRID 361305 반응식
[N+:1]([CH:4]1[CH:9]([C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[C:12]([O:18][CH3:19])[CH:11]=2)[CH2:8][CH:7]=[CH:6][CH2:5]1)([O-:3])=[O:2].[H][H]>C(OCC)(=O)C.[Pd]>[N+:1]([CH:4]1[CH2:5][CH2:6][CH2:7][CH2:8][CH:9]1[C:10]1[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[C:12]([O:18][CH3:19])[CH:11]=1)([O-:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 13970723HCID 13970723, 화합물HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 537264301-Nitro-2-(3,4-dimethoxyphenyl)cyclohexane수율 91%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

To 10 mmol of 4-nitro-5-(3,4-dimethoxyphenyl)cyclohexene in 100 mL of ethyl acetate was added 200 mg of 10% palladium on carbon. The resulting suspension was shaken at 50 psi of hydrogen on a Parr Apparatus for one hour. The catalyst was removed by filtration through Celite® diatomaceous earth and the filtrate evaporated to dryness in vacuo to give a 91% yield of the desired product based on 1H NMR.

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후처리

  1. customThe catalyst was removed by filtration through Celite® diatomaceous earth
  2. customthe filtrate evaporated to dryness in vacuo

출처 및 근거

ORD 기록
ord-0e0f383153a34c4e82c638329390a76c
출처 데이터셋
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05866513

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